Department of Dermatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Department of Diabetes and Endocrinology, Hokkaido P.W.F.A.C. Sapporo Kosei General Hospital, Sapporo, Japan.
Front Immunol. 2019 Jun 26;10:1439. doi: 10.3389/fimmu.2019.01439. eCollection 2019.
Anti-hyperglycemic drug dipeptidyl peptidase-IV inhibitors (DPP-4i) have recently been recognized as bullous pemphigoid (BP) inducing drugs. It remains uncertain whether DPP-4i induce BP-IgG autoantibodies before the onset of BP. To evaluate the effect of DPP-4i in the development of BP-IgG autoantibodies in type 2 diabetes mellitus (T2DM) patients. A cross-sectional study on 221 DPP-4i (+) and 54 DPP-4i (-) T2DM cases was conducted. BP180 NC16A, BP230, and full-length BP180 ELISAs were used to detect the BP-IgG autoantibodies. We have also statistically analyzed the proportion of age, gender, intake periods of DPP-4i, and hemoglobin A1c level between anti-full-length BP180 IgG-positive and -negative DPP-4i (+) T2DM cases to identify co-founding factors. BP180 NC16A ELISA, BP230 ELISA, and full-length BP180 ELISA were positive in 1.8, 2.2, and 10.9% of DPP-4i (+) T2DM cases, respectively; in contrast, they were positive in 0, 7.4, and 5.6% of DPP-4i (-) T2DM cases, respectively. The odds ratio for the development of BP-IgG autoantibodies detected by full-length BP180 ELISA was 2.070 for DPP-4i (+). There were no significant differences between the genders, intake periods of DPP-4i, nor of hemoglobin A1c levels, the anti-full-length BP180 IgG-positive cases tended to be significantly older than anti-full-length BP180 IgG-negative cases (median 74 vs. 69, = 0.025) in the DPP-4i (+) T2DM cases. We focused the analysis on DPP-4i intake and not on the effects of metformin and other drugs. Exposure to specific DPP-4i may induce the development of anti-full-length BP180 autoantibodies even in T2DM patients without any clinical symptoms of BP. Aging would be a risk factor to develop anti-full-length BP180-IgG autoantibody in DPP-4i (+) T2DM cases.
二肽基肽酶-4 抑制剂(DPP-4i)最近被认为是大疱性类天疱疮(BP)的诱导药物。在 BP 发病前,DPP-4i 是否会诱导 BP-IgG 自身抗体,目前仍不确定。本研究旨在评估 DPP-4i 在 2 型糖尿病(T2DM)患者 BP-IgG 自身抗体发展中的作用。采用横断面研究,纳入 221 例 DPP-4i(+)和 54 例 DPP-4i(-)T2DM 患者。采用 BP180 NC16A、BP230 和全长 BP180 ELISA 检测 BP-IgG 自身抗体。我们还对 DPP-4i(+)T2DM 患者中全长 BP180 IgG 阳性和阴性的年龄、性别、DPP-4i 摄入时间和糖化血红蛋白(HbA1c)水平比例进行了统计学分析,以确定混杂因素。DPP-4i(+)T2DM 患者中,BP180 NC16A ELISA、BP230 ELISA 和全长 BP180 ELISA 的阳性率分别为 1.8%、2.2%和 10.9%;相比之下,DPP-4i(-)T2DM 患者的阳性率分别为 0%、7.4%和 5.6%。全长 BP180 ELISA 检测到的 BP-IgG 自身抗体的发展的优势比(OR)为 DPP-4i(+)的 2.070。DPP-4i(+)T2DM 患者中,性别、DPP-4i 摄入时间和 HbA1c 水平之间无显著差异,全长 BP180 IgG 阳性患者的年龄明显大于全长 BP180 IgG 阴性患者(中位数 74 岁 vs. 69 岁,=0.025)。我们将分析重点放在 DPP-4i 的摄入上,而不是二甲双胍和其他药物的作用上。在没有任何 BP 临床症状的 T2DM 患者中,暴露于特定的 DPP-4i 可能会诱导全长 BP180 自身抗体的产生。在 DPP-4i(+)T2DM 患者中,年龄增长是产生全长 BP180-IgG 自身抗体的危险因素。